Orphanet: Molecular diagnosis of Achondrogenesis type 1B SLC26A2 gene

Search for a diagnostic test

* (*) mandatory field

Molecular diagnosis of Achondrogenesis type 1B (SLC26A2 gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 01/06/2015
  • Phone : +31 (0)43 387 1345
  • Additional Phone : +31 (0)43 387 1272
  • Fax : +31 (0)43 387 7901
  • Website
  • Contact
Last update: June 2015

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Molecular genetics

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (1)
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.